(Q32142983)
English
hereditary spastic paraplegia 3A
hereditary spastic paraplegia that is characterized by lower limb weakness and spasticity that is generally non-progressive or extremely slow and has material basis in mutation in the ATL1 gene on chromosome 14q22
- FSP1
- autosomal dominant spastic paraplegia 3
- strumpell disease
- autosomal dominant spastic paraplegia type 3
- autosomal dominant familial spastic paraplegia 1
- SPG3A
- Familial Spastic Paraplegia, Autosomal Dominant, 1
- Spg3
- hereditary spastic paraplegia type 3A
- SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT; SPG3A
- StrC<mpell disease
- SPASTIC PARAPLEGIA 3, AUTOSOMAL DOMINANT
- Strümpell disease
Statements
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C142893
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Identifiers
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